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|The Matthews Consultancy|
European pharmaceutical/biotech consultancy specializing in project management, medical writing, and business development.
A quality assurance, regulatory, and clinical consulting firm providing services to the medical device, pharmaceutical and food industries.
|MedFO, Inc. - Medical Information Communication Consulting|
Specialty consulting firm that focuses almost exclusively upon the strategy, operations, and functions of departments that fall under the Medical Affairs umbrella.
|Medical device consultants|
Consultants for FDA and internationally regulated medical device firms, specializing in submissions, compliance, warning letter responses, inspection responses, quality system compliance, auditing and training
|Medical Device Consultants, Inc. (MDCI)|
provides worldwide regulatory, clinical, and quality assurance consulting services to medical device and diagnostic product manufacturers to meet US, Canadian, and European requirements.
|Medical Device Technology Consultants - Cambridge UK|
MDTc is an independent consultancy to the medical devices industry. Based near Cambridge, England, MDTc helps bring products to market and comply with regulatory requirements.
|Medical Devices Consulting|
Regulatory affairs, quality assurance, custom software, and compliance contracting and consulting services.
|MediQuest Associates, Inc.|
Pharmaceutical and regulatory specialists providing drug data analysis, coding assistance, regulatory affairs and pharmaceutical classification services.
|Medius AG - Drug Regulatory Affairs and Development|
Medius is a consulting and service company based in Switzerland, engaged in regulatory affairs of pharmaceuticals, medical devices, and in vitro diagnostics.
German consultant for the pharmaceutical industry.
|Milestone Biomedical Associates|
A contract consulting services organization specializing in the nonclinical product development of drugs, biologics, and medical devices.
Pharmaceutical Compliance Services, Inc. prepares domestic and international pharmaceutical manufacturing sites for FDA Regulatory Pre-Approval Inspections (PAIs) and routine FDA inspections. PCS specializes in providing “Quality Systems” audits and cGMP gap analysis/risk assessment guidance.
|New World Regulatory Solutions/SOOP International|
Regulatory, quality and technical affairs guidance for international medical diagnostic device manufacturers.
|Newland GxP Consultancy|
European pharmaceutical GxP Consultancy.
|Northvail Consulting - specializing in HIPAA compliance|
Northvail Consulting provides HIPAA privacy and security compliance services to healthcare providers in Colorado and the surrounding region.
Using an electronic submission system (eSub), Octagon assists clients in the achievement an approved regulatory submission.
|Online HIPAA training|
Online training for HIPAA compliance for insurance professionals.
|Pensa Technology Solutions Inc.|
21 cfr part 11 regulatory compliance of FDA pharmaceutical GMP validation for ERP life sciences computer information systems.
|Perkins and Perkins|
FDA consultants Perkins and Perkins, Inc. conduct mock FDA audits to insure Good Clinical Practice (GCP) compliance, quality assurance and FDA audit preparation.
|Peter McCay - Consulting Engineers Limited|
A qualified control and instrument C&I commissioning engineer, with more than 28 years professional experience in the pharmaceutical, nuclear, petro chemical and process industries, predomininantly with major operating manufacturing companies